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Items: 1 to 20 of 184

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7049711inversion1nstd229human GRCh38 chr7: 57,268,545-57,328,043 , GRCh37.p13 chr7|NW_003571038.1: 1-53,524 , GRCh37.p13 chr7: 57,342,227-57,395,750 LOC100419779
    nsv7047413inversion1nstd229human GRCh38 chr7: 57,270,375-57,280,451 , GRCh37.p13 chr7: 57,342,227-57,348,158 , GRCh37.p13 chr7|NW_003571038.1: 1-5,932 LOC100419779
    nsv6835880copy number variation1nstd229human GRCh38 chr7: 57,274,614-57,279,061 , GRCh37.p13 chr7: 57,342,321-57,346,768 , GRCh37.p13 chr7|NW_003571038.1: 95-4,542 LOC100419779
    nsv6821805copy number variation1nstd229human GRCh38 chr7: 57,225,602-57,408,229 , GRCh37.p13 chr7: 57,342,227-57,475,935 , GRCh37.p13 chr7|NW_003571038.1: 1-133,710 MIR3147, LOC105375299, 4 more genes
    nsv6634332copy number variation1nstd102humanUncertain significance GRCh37 chr7: 113,371-159,042,325 , GRCh38.p12 chr7: 113,371-159,249,635 RRBP1P1, SLC29A4P1, 2680 more genes
    nsv6632160copy number variation1nstd224human GRCh37 chr7: 57,291,189-57,460,667 , GRCh38.p12 chr7: 57,223,482-57,392,960 LOC100419779, LOC105375298, 1 more genes
    nsv6632159copy number variation1nstd224human GRCh37 chr7: 57,256,128-57,881,608 , GRCh38.p12 chr7: 57,188,421-57,821,902 VN1R29P, LOC100419779, 24 more genes
    nsv6631972copy number variation1nstd224human GRCh37 chr7: 57,188,377-57,531,189 , GRCh38.p12 chr7: 57,120,670-57,471,483 GUSBP10, MTND5P6, 30 more genes
    nsv6631905copy number variation1nstd224human GRCh37 chr7: 57,269,842-57,878,853 , GRCh38.p12 chr7: 57,202,135-57,819,147 LOC100420545, LOC105375299, 16 more genes
    nsv6611657copy number variation1nstd223human GRCh38 chr7: 57,185,639-57,823,151 , GRCh37.p13 chr7: 57,253,346-57,882,857 LOC105375300, MTCO3P4, 27 more genes
    nsv6606927copy number variation1nstd223human GRCh38 chr7: 57,271,701-57,272,900 , GRCh37.p13 chr7: 57,339,408-57,340,607 LOC100419779
    nsv6606751copy number variation1nstd223human GRCh38 chr7: 57,254,109-57,308,355 , GRCh37.p13 chr7|NW_003571038.1: 1-33,836 , GRCh37.p13 chr7: 57,342,227-57,376,062 LOC100419779
    nsv6315223complex substitution1nstd102humanPathogenic GRCh37 chr7: 43,360-159,119,707 , GRCh38.p12 chr7: 43,360-159,327,017 AOC1, ACHE, 2682 more genes
    nsv6137008copy number variation1nstd213human GRCh37 chr7: 57,340,000-57,610,001 , GRCh38.p12 chr7: 57,272,293-57,550,295 SAPCD2P2, LOC100419779, 8 more genes
    nsv6136194copy number variation1nstd213human GRCh37 chr7: 57,300,000-57,460,001 , GRCh38.p12 chr7: 57,232,293-57,392,294 LOC100419779, LOC105375298
    nsv6014919copy number variation1nstd212human GRCh38 chr7: 57,274,648-57,279,248 , GRCh37.p13 chr7|NW_003571038.1: 129-4,729 , GRCh37.p13 chr7: 57,342,355-57,346,955 LOC100419779
    nsv5556846sequence alteration1nstd206human GRCh38 chr7: 2,511,247-157,318,976 , GRCh37.p13 chr7: 2,550,881-157,111,670 , AHR, 2675 more genes
    nsv5482153copy number variation1nstd206human GRCh38 chr7: 56,993,800-57,540,242 , GRCh37.p13 chr7: 57,190,580-57,599,948 , MTCYBP29, 39 more genes
    nsv5039775inversion1nstd200human GRCh38 chr7: 22,938,090-134,148,361 , GRCh37.p13 chr7: 22,977,709-133,833,114 , NFE4, 1832 more genes
    nsv4964675copy number variation1nstd200human GRCh38 chr7: 57,185,639-57,823,153 , GRCh37.p13 chr7: 57,253,346-57,882,859 LOC105375297, GUSBP12, 27 more genes
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